Canonical Allele Identifier: CA1339333033
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240872927A= , CM000664.2:g.240872927A= GRCh38
NC_000002.11:g.241812344A= , CM000664.1:g.241812344A= GRCh37
NC_000002.10:g.241461017A= NCBI36
NG_008005.1:g.9183A=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.525-52A= MANE Select ENSP00000302620.3:n.525-52A=
ENST00000307503.3:c.525-52A= ENSP00000302620.3:n.525-52A=
ENST00000472436.1:n.545-52A=
ENST00000476698.1:n.262-52A=
NM_000030.2:c.525-52A= NP_000021.1:n.525-52A=
NM_000030.3:c.525-52A= MANE Select NP_000021.1:n.525-52A=